ic Specialist II

Main responsibilities: 
Be responsible for the reception, counting, labeling and verification of specimens, and ensure the accurate input of specimen information into the system as well as the effective distribution of specimens.  
Secondary work: Assist in assembling and inspecting the sampling and testing kits to ensure quality control.  
Document Management: Responsible for the scanning and archiving of documents related to the management of case specimens.
Environmental maintenance: Keep the sample management area clean and orderly.  
Teamwork: Complete other related tasks assigned by the supervisor.  

Personal trait requirements:  
Carefulness and patience  
Strong sense of responsibility  
Good English proficiency (TOEIC 550 or above, IELTS 4.5 or above or equivalent level)  
Teamwork spirit and good logical thinking

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.
Our team members are passionate about what we do, but we understand work is only one of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.
We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.

We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to talking to you about working at Novotech.